"0536-1232-01" National Drug Code (NDC)

NDC Code	0536-1232-01
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (0536-1232-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC	0536-1232
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Aspirin
Proprietary Name Suffix	Regular Strength
Non-Proprietary Name	Aspirin
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20190601
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M013
Manufacturer	Rugby Laboratories
Substance Name	ASPIRIN
Strength	325
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]